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1 membrane proteins together with PAGFP-tagged clathrin light chain.
2 ed alone or with photoactivatable GFP-tagged clathrin light chain.
3 or the S3 path as an interaction surface for clathrin light chain.
4 ) that includes residues crucial for binding clathrin light chain.
5 ith clathrin-mediated endocytosis, including clathrin light chain.
6 r interaction with the conserved sequence of clathrin light chains.
7 avy chain subunits nor bind significantly to clathrin light chains.
8 lize with the plant plasma membrane and with CLATHRIN LIGHT CHAIN 1, a component of clathrin-mediated
9  B. cinerea EV marker BcPLS1 and Arabidopsis CLATHRIN LIGHT CHAIN 1, one of the core components of CC
10 isms, as well as Retinitis Pigmentosa Type 2-Clathrin Light Chain, a membrane protein with a novel do
11             Furthermore, dissociation of the clathrin light chain, a protein that plays major role in
12 ns of beta-actin, occludin, claudin-1, ZO-1, clathrin light chain A1, and caveolin-1 were imaged by t
13                     AFL1 colocalization with clathrin light chain along the plasma membrane, together
14 re clathrin-mediated endocytosis and labeled clathrin light chain also displayed altered localization
15 an Hip1 and Hip1R and their interaction with clathrin light chain and actin were analyzed.
16 he membrane recruitment of PIPKbeta and both clathrin light chain and dynamin.
17 ating with slightly different affinities for clathrin light chain and more markedly with effects of c
18 =200 nm clusters of transferrin receptor and clathrin light chain at < or =25 nm resolution and confi
19 thrin-coated vesicles and to colocalize with clathrin light chain at putative sites of endocytosis at
20 n overlaps the domain putatively involved in clathrin light chain binding and is adjacent to the heav
21                                              Clathrin light chain binding induced a compact conformat
22 ight chain and more markedly with effects of clathrin light chain binding on Hip protein-actin intera
23 HIPR-1 mutants demonstrated that neither the clathrin light chain-binding domain nor the clathrin hea
24                     The coiled-coil domains (clathrin light chain-binding) of Hip1 and Hip1R were fou
25 revealed two conformations of the regulatory clathrin light chain bound to clathrin heavy chain.
26  dynamin K44A, epsin 2a, amphiphysin A1, and clathrin light chain but enhanced by that for the active
27   Expression of FK506 binding protein (FKBP)-clathrin light chain chimeras, to inhibit clathrin membr
28 icle is the clathrin triskelion, composed of clathrin light chain (Clc) and clathrin heavy chain (Chc
29                                 To establish clathrin light chain (CLC) function in vivo, we engineer
30                                  The role of clathrin light chain (CLC) in clathrin-mediated endocyto
31 termine Chc trimerization and binding to the clathrin light chain (Clc) subunit.
32                                              Clathrin light chain (CLC) subunits in vertebrates are e
33                                          The clathrin light chain (CLC) subunits participate in sever
34  Three clathrin heavy chains associated with clathrin light chains (CLC) assemble into triskelia that
35           The phosphorylation state of yeast clathrin light chain (Clc1p) in vivo was monitored by [3
36                                              Clathrin light chains (CLCa and CLCb) are major constitu
37 f three clathrin heavy chains and associated clathrin light chains (CLCs).
38                          LatB decreased AFL1-Clathrin Light Chain colocalization, further indicating
39      In vivo overexpression of a fragment of clathrin light chain comprising the Hip1R-binding region
40          HIP1 and HIP12/1R interact with the clathrin light chain EED regulatory site and stimulate c
41 in CLC1-knockout yeast, which indicates that clathrin light chain facilitates the transition from the
42 tic perturbation of clathrin function with a clathrin light chain-FKBP chimera oligomerizable by the
43 at the cell cortex, which colocalized with a clathrin light chain fluorescent fusion protein (CLC-FFP
44                                 In contrast, clathrin light chain genes (CLTA and CLTB) apparently ar
45 alcyon cytosolic domain as bait, we isolated clathrin light chain in a yeast two-hybrid screen.
46  pits labeled with green fluorescent protein-clathrin light chains in HeLa cells show that even when
47                                          Two clathrin light chain isoforms, CLCa and CLCb, are integr
48 t, real-time analysis of Hip1R-YFP and DsRed-clathrin light chain (LC) in live cells revealed that th
49 ggests the mode of binding between sla2p and clathrin light chain may be different in yeast.
50 ime with plasma membrane domains enriched in clathrin light-chain molecules.
51 rectly detected that PI4KIIbeta comoves with clathrin light chain on vesicles.
52 us does not appear to colocalize with either clathrin light chain or caveolin-1 by immunofluorescence
53 croscopy using fluorescent proteins fused to clathrin light chain or GLUT4 reveals these structures a
54                                  The role of clathrin light chain phosphorylation in regulating clath
55                                              Clathrin light chain subunits (LCa and LCb) contribute t
56 ents of the clathrin heavy chain, which bind clathrin light-chain subunits and mimic the self-assembl
57 trolled by only three acidic residues in the clathrin light-chain subunits.
58                                        Using clathrin light chain (TcCLC) and EpsinR (TcEpsinR) as af
59  foci overlap with those formed by DRP1C and clathrin light chain, there are clear differences in beh
60 ows the observed conformational variation in clathrin light chains to alter the conformation of the c
61 ll cycle, a cell line expressing SNAP-tagged clathrin light chains was generated.